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234353009: Congenital transferrin deficiency (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
351093011 Congenital transferrin deficiency en Synonym Active Entire term case insensitive SNOMED CT core module
622660011 Congenital transferrin deficiency (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module


1 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Congenital transferrin deficiency Is a Microcytic anemia true Inferred relationship Existential restriction modifier
Congenital transferrin deficiency Finding site Erythrocyte false Inferred relationship Existential restriction modifier
Congenital transferrin deficiency Finding site Hematopoietic system structure false Inferred relationship Existential restriction modifier
Congenital transferrin deficiency Has definitional manifestation Erythropenia false Inferred relationship Existential restriction modifier
Congenital transferrin deficiency Has definitional manifestation Microcytosis, red cells false Inferred relationship Existential restriction modifier
Congenital transferrin deficiency Finding site Hematopoietic system structure false Inferred relationship Existential restriction modifier
Congenital transferrin deficiency Is a Congenital anomaly of the hematopoietic system false Inferred relationship Existential restriction modifier
Congenital transferrin deficiency Occurrence Congenital true Inferred relationship Existential restriction modifier 3
Congenital transferrin deficiency Is a Congenital anemia true Inferred relationship Existential restriction modifier
Congenital transferrin deficiency Is a Anemia due to disturbance of hemoglobin synthesis true Inferred relationship Existential restriction modifier
Congenital transferrin deficiency Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier
Congenital transferrin deficiency Is a Hereditary red blood cell disorder false Inferred relationship Existential restriction modifier
Congenital transferrin deficiency Is a Congenital disease false Inferred relationship Existential restriction modifier
Congenital transferrin deficiency Has interpretation Below reference range true Inferred relationship Existential restriction modifier 1
Congenital transferrin deficiency Has interpretation Below reference range true Inferred relationship Existential restriction modifier 2
Congenital transferrin deficiency Interprets Red blood cell count true Inferred relationship Existential restriction modifier 1
Congenital transferrin deficiency Interprets Measurement of total hemoglobin concentration true Inferred relationship Existential restriction modifier 2
Congenital transferrin deficiency Interprets Red blood cell size determination true Inferred relationship Existential restriction modifier 4

Inbound Relationships Type Active Source Characteristic Refinability Group
Congenital atransferrinemia Is a True Congenital transferrin deficiency Inferred relationship Existential restriction modifier

This concept is not in any reference sets

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